HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110575368C>T , CM000672.2:g.110575368C>T | GRCh38 |
NC_000010.10:g.112335126C>T , CM000672.1:g.112335126C>T | GRCh37 |
NC_000010.9:g.112325116C>T | NCBI36 |
NG_012217.1:g.12678C>T , LRG_774:g.12678C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000684988.1:n.296C>T | ||
ENST00000687823.1:n.77C>T | ||
ENST00000689932.1:n.2226C>T | ||
ENST00000691297.1:n.296C>T | ||
ENST00000691527.1:n.253C>T | ||
ENST00000692792.1:n.282C>T | ||
ENST00000361804.5:c.163C>T MANE Select | ENSP00000354720.5:p.His55Tyr | |
ENST00000361804.4:c.163C>T | ENSP00000354720.4:p.His55Tyr | |
ENST00000462899.1:n.309C>T | ||
NM_005445.3:c.163C>T , LRG_774t1:c.163C>T | NP_005436.1:p.His55Tyr | |
NM_005445.4:c.163C>T MANE Select | NP_005436.1:p.His55Tyr |